Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Apr;10(2):171-187.
doi: 10.1007/s12687-018-0394-0. Epub 2018 Nov 7.

What do people think about genetics? A systematic review

Affiliations
Review

What do people think about genetics? A systematic review

Erin LePoire et al. J Community Genet. 2019 Apr.

Abstract

Genetics is increasingly becoming a part of modern medical practice. How people think about genetics' use in medicine and their daily lives is therefore essential. Earlier studies indicated mixed attitudes about genetics. However, this might be changing. Using the preferred reporting items for systematic reviews and meta-analyses (PRISMA) as a guideline, we initially reviewed 442 articles that looked at awareness, attitudes, knowledge, and perception of risks among the general and targeted recruitment populations. After fitting our criteria (from the last 5 years, conducted in the USA, non-provider populations, quantitative results reported, and assessed participants 18 years and older), finally 51 eligible articles were thematically coded and presented in this paper. Awareness is reported as relatively high in the studies reviewed. Attitudes are mixed but with higher proportions reporting positive attitudes towards genetic testing and counseling. Self-reported knowledge is reasonably high, specifically with the effects of specific programs developed to raise knowledge levels of the general and targeted recruited populations. Perception of risk is somewhat aligned with actual risk. With the reasonable positive reports of genetic awareness and knowledge, there is similar positive attitude and perception of risk, supporting the need for continued dissemination of such knowledge. Given interest in incorporating community participation in genomic educational strategies, we provide this review as a baseline from which to launch community-specific educational supports and tools.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest

Erin LePoire, Deborah Bowen, Lorelei Walker, and Bashakhi Basu declare that they have no conflicting interests.

Ethical approval

This article does not contain any studies with human or animal subjects performed by any of the authors.

Figures

Fig. 1
Fig. 1
PRISMA 2009 flow diagram

Similar articles

Cited by

References

    1. Adams HR, Rose K, Augustine EF, Kwon JM, deBlieck EA, Marshall FJ, Vierhile A, Mink JW, Nance MA. Experience, knowledge, and opinions about childhood genetic testing in batten disease. Mol Genet Metab. 2014;111(2):197–202. - PMC - PubMed
    1. Agurs-Collins T, Ferrer R, Ottenbacher A, Waters EA, O’Connell ME, Hamilton JG. Public awareness of direct-to-consumer genetic tests: findings from the 2013 U.S. Health Information National Trends Survey. J Cancer Educ. 2015;30(4):799–807. - PMC - PubMed
    1. Allain DC, Friedman S, Senter L. Consumer awareness and attitudes about insurance discrimination post-enactment of the Genetic Information Nondiscrimination Act. Familial Cancer. 2012;11(4):637–644. - PubMed
    1. Allyse M, Sayres LC, Goodspeed TA, Cho MK. Attitudes towards non-invasive prenatal testing for aneuploidy among US adults of reproductive age. J Perinatol. 2014;34(6):429–434. - PMC - PubMed
    1. Andersen MR, Thorpe J, Buist DS, et al. Cancer risk awareness and concern among women with a family history of breast or ovarian cancer. Behav Med (Washington, DC) 2016;42(1):18–28. - PMC - PubMed

LinkOut - more resources